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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051311inversion1nstd229human GRCh38 chr2: 101,647,680-105,928,217 , GRCh37.p13 chr2: 102,264,142-106,544,673 LOC107985929, SLC9A2, 57 more genes
    nsv6692171copy number variation1nstd229human GRCh38 chr2: 102,211,388-102,443,779 , GRCh37.p13 chr2: 102,827,848-103,060,239 IL18R1, MIR4772, 5 more genes
    nsv6636875copy number variation1nstd102humanUncertain significance GRCh37 chr2: 102,443,532-105,019,078 , GRCh38.p12 chr2: 101,827,070-104,402,620 IL1RL2, LOC107985926, 27 more genes
    nsv6636232copy number variation1nstd102humanUncertain significance GRCh37 chr2: 102,579,520-103,179,707 , GRCh38.p12 chr2: 101,963,058-102,563,248 MIR4772, IL1RL2, 10 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6352981copy number variation1nstd223human GRCh38 chr2: 102,127,822-102,717,507 , GRCh37.p13 chr2: 102,744,282-103,333,966 CFAP144P2, SLC9A2, 9 more genes
    nsv6349211copy number variation1nstd223human GRCh38 chr2: 102,073,096-102,703,088 , GRCh37.p13 chr2: 102,689,556-103,319,547 SLC9A2, IL1RL2, 8 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6291008copy number variation1nstd102humanUncertain significance GRCh37 chr2: 101,699,537-106,383,710 , GRCh38.p12 chr2: 101,083,075-105,767,253 C2orf49, LINC01870, 71 more genes
    nsv6134605copy number variation1nstd213human GRCh37 chr2: 101,700,000-103,280,001 , GRCh38.p12 chr2: 101,083,538-102,663,542 IL1R1, SLC9A2, 27 more genes
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5446507copy number variation1nstd206human GRCh38 chr2: 102,410,668-102,410,726 , GRCh37.p13 chr2: 103,027,128-103,027,186 SDR42E1P5
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4463300mobile element insertion1nstd166human GRCh37.p13 chr2: 103,028,089-103,028,089 , GRCh38.p12 chr2: 102,411,629-102,411,629 SDR42E1P5
    nsv4454805copy number variation1nstd102humanUncertain significance GRCh37 chr2: 102,917,327-106,755,564 , GRCh38.p12 chr2: 102,300,867-106,139,108 LOC105373521, LOC107985927, 53 more genes
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